hai ha nguyen
hai ha nguyen
Vietnam Institute of Genome Research
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Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators
A Fujimoto, Y Totoki, T Abe, KA Boroevich, F Hosoda, HH Nguyen, M Aoki, ...
Nature genetics 44 (7), 760-764, 2012
Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity
A Fujimoto, M Furuta, Y Shiraishi, K Gotoh, Y Kawakami, K Arihiro, ...
Nature communications 6 (1), 6120, 2015
IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility
H Ha Nguyen, R Takata, S Akamatsu, D Shigemizu, T Tsunoda, ...
Human molecular genetics 21 (9), 2076-2085, 2012
Complete human mtDNA genome sequences from Vietnam and the phylogeography of Mainland Southeast Asia
NT Duong, E Macholdt, ND Ton, L Arias, R Schröder, N Van Phong, ...
Scientific Reports 8 (1), 11651, 2018
Regulation of dendritic cell function by insulin/IGF-1/PI3K/Akt signaling through klotho expression
NT Xuan, NH Hoang, VP Nhung, NT Duong, NH Ha, NV Hai
Journal of Receptors and Signal Transduction 37 (3), 297-303, 2017
Single nucleotide and structural variants of CYP2D6 gene in Kinh Vietnamese population
HH Nguyen, TTH Ma, NP Vu, QTN Bach, TH Vu, TD Nguyen, H Van Nong
Medicine 98 (22), 2019
Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure
ND Ton, H Nakagawa, NH Ha, NT Duong, VP Nhung, LTT Hien, HTT Hue, ...
Human Mutation 39 (10), 1384-1392, 2018
CYP2C19 genetic polymorphism in the Vietnamese population
NP Vu, HTT Nguyen, NTB Tran, TD Nguyen, HTT Huynh, XT Nguyen, ...
Annals of Human Biology 46 (6), 491-497, 2019
Mutational screening of germline RB1 gene in Vietnamese patients with retinoblastoma reveals three novel mutations
HH Nguyen, HTT Nguyen, NP Vu, QT Le, CM Pham, TT Huyen, H Manh, ...
Molecular vision 24, 231, 2018
Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early‐onset Parkinson’s disease
ND Ton, ND Thuan, MTH Thuong, TTB Ngoc, VP Nhung, NTT Hoa, ...
Molecular genetics & genomic medicine 8 (10), e1463, 2020
Host Genetic Risk Factors Associated with COVID-19 Susceptibility and Severity in Vietnamese
VP Nhung, ND Ton, TTB Ngoc, MTH Thuong, NTT Hai, KTP Oanh, ...
Genes 13 (10), 1884, 2022
Polymorphic analysis of CYP2C9 gene in Vietnamese population
NP Vu, TTH Ma, NTB Tran, HTT Huynh, TD Nguyen, DT Nguyen, ...
Molecular biology reports 45, 893-900, 2018
Genome sequence of a Vietnamese Bacillus thuringiensis strain TH19 reveals two potential insecticidal crystal proteins against Etiella zinckenella larvae
PLB Hang, NN Linh, NH Ha, N Van Dong
Biological Control 152, 104473, 2021
Whole genome sequencing of a Vietnamese family from a dioxin contamination hotspot reveals novel variants in the son with undiagnosed intellectual disability
DT Nguyen, HH Nguyen, TD Nguyen, TTH Nguyen, K Nakano, K Maejima, ...
International Journal of Environmental Research and Public Health 15 (12), 2629, 2018
Đa hình đơn bội DNA ty thể của các cá thể người Việt Nam
NĐ Tôn, NTT Linh, VH Chi, TTN Diệp, ĐTK Hương, BT Tuyết, NH Hà, ...
Tạp chí Công nghệ sinh học 6 (4), 579-590, 2008
Novel mutations of the PAX6, FOXC1, and PITX2 genes cause abnormal development of the iris in Vietnamese individuals
HH Nguyen, CM Pham, HTT Nguyen, NP Vu, TT Duong, TD Nguyen, ...
Molecular Vision 27, 555-563, 2021
Genetic variation of mitochondrial sequence-hv2 in Vietnamese populations
NH Ha, PN Khoi, VP Nhung, N Van Phong, NT Duong, N Van Hai, ...
Academia Journal of Biology 38 (2), 243-249, 2016
Mutational analysis of GJB2, GJB6 and 12S rRNA genes in Vietnamese non-syndromic deaf children
NT Duong, NT Xuan, NH Ha, ND Ton, HTT Hue, PTT Trang, DTT Ha, ...
Asian Journal of Biomedical and Pharmaceutical Sciences, 02, 2015
Single Nucleotide Polymorphisms of ADH1B, ADH1C and ALDH2 Genes in 235 People Living in Thai Nguyen Province of Vietnam
YTT Hoang
Asian Pacific Journal of Cancer Prevention 23 (12), 4243-4251, 2022
Novel and very rare causative variants in the COL7A1 gene of Vietnamese patients with recessive dystrophic epidermolysis bullosa revealed by whole‐exome …
THT Ma, TLA Luong, TL Hoang, TTH Nguyen, TH Vu, VK Tran, ...
Molecular Genetics & Genomic Medicine 9 (8), e1748, 2021
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